DE191855C - - Google Patents
Info
- Publication number
- DE191855C DE191855C DENDAT191855D DE191855DA DE191855C DE 191855 C DE191855 C DE 191855C DE NDAT191855 D DENDAT191855 D DE NDAT191855D DE 191855D A DE191855D A DE 191855DA DE 191855 C DE191855 C DE 191855C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- solution
- anthroxanoic
- finely divided
- nitrosomandelic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000002253 acid Substances 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 11
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- DNNLQTCPOLHGIQ-UHFFFAOYSA-N 2-hydroxy-2-(2-nitrophenyl)acetic acid Chemical class OC(=O)C(O)C1=CC=CC=C1[N+]([O-])=O DNNLQTCPOLHGIQ-UHFFFAOYSA-N 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- QDHHCQZDFGDHMP-UHFFFAOYSA-O chloroamine;hydron Chemical compound Cl[NH3+] QDHHCQZDFGDHMP-UHFFFAOYSA-O 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 239000000706 filtrate Substances 0.000 claims 1
- 150000002828 nitro derivatives Chemical class 0.000 claims 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims 1
- -1 nitrosomandelic acid Chemical group 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- JXDYKVIHCLTXOP-UHFFFAOYSA-N Isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/20—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE191855C true DE191855C (pl) |
Family
ID=455228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT191855D Active DE191855C (pl) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE191855C (pl) |
-
0
- DE DENDAT191855D patent/DE191855C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE191855C (pl) | ||
DE493025C (de) | Verfahren zur Darstellung von o-Arylaminorhodanverbindungen | |
DE611258C (de) | Anreibeversilberungsmittel | |
DE1081880B (de) | Verfahren zur Herstellung von Titan(III)-acetylacetonat | |
DE189179C (pl) | ||
AT96688B (de) | Verfahren zur Darstellung von neuen aromatischen Carbonylverbindungen mit dreiwertigem Arsen. | |
DE611693C (de) | Verfahren zur Darstellung des Hexamethylentetraminbetains | |
DE859311C (de) | Verfahren zur Darstellung von 1, 3-Dimethyl-4-amino-5-formylamino-2, 6-dioxypyrimidin aus 1, 3-Dimethyl-4-amino-5-nitroso-2, 6-dioxypyrimidin | |
DE424217C (de) | Verfahren zur Herstellung von Reduktionsprodukten der 2,3-Oxynaphthoesaeurenitroarylide | |
DE526392C (de) | Verfahren zur Herstellung von Metallkomplexverbindungen | |
DE718170C (de) | Verfahren zur Herstellung von kupferhaltigem Bleipulver | |
AT153500B (de) | Verfahren zur Herstellung von Verbindungen der Sulfhydrylkeratinsäure. | |
DE184693C (pl) | ||
DE362984C (de) | Verfahren zur Darstellung von Derivaten des 1,1-Dianthrachinonyls | |
DE330813C (de) | Verfahren zur Darstellung von Alkoholen und Aminoalkoholen der Chinolinreihe | |
DE467423C (de) | Verfahren zur Herstellung fuer die Farblackbereitung geeigneter eisenhaltiger innerer Komplexverbindungen | |
DE676802C (de) | Herstellung von schwer loeslichem Zinkgelb | |
DE206344C (pl) | ||
DE564215C (de) | Verfahren zur Darstellung von Thioderivaten der Phenole | |
DE450285C (de) | Verfahren zum Reinigen von Zinklaugen neutraler oder alkalischer Reaktion von Schwer- metallverunreinigungen, wie Kupfer, Blei, Cadmium, Nickel, unter Ausschluss von Eisen | |
AT157699B (de) | Varfahren zur Darstellung wasserlöslicher organischer Quecksilberverbindungen. | |
DE182217C (pl) | ||
DE911544C (de) | Verfahren zur Herstellung hochschwefelhaltiger Stoffe | |
DE459602C (de) | Verfahren zur Darstellung von Glykolsaeure und ihren Derivaten | |
DE205450C (pl) |